# STERIMED, Inc. – FDA Inspection, Dec 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/sterimed-inc/e660d864-83a2-4933-8266-900b541b09ba
Source feed: FDA_Inspections

> FDA inspection 996126 of STERIMED, Inc., December 14, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996126
- Company Name: STERIMED, Inc.
- Inspection Date: 2016-12-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 850702 - 2013-09-27
- FDA Inspection 638180 - 2010-01-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/samuel-l-murray/74b03eba-03ee-409b-9394-8e903adf6288)

Company: https://www.keypedia.com/companies/sterimed-inc/699ab6a1-3094-4076-97f1-799cc072234c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7